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Neisseria meningitidis capsular polysaccharide antigen (serogroups A, C, W, Y) (null)

Target
null
Molecular classification
Polysaccharide antigen, Bacterial capsular antigen, Vaccine antigen
01

Overview

The Neisseria meningitidis capsular polysaccharide antigens of serogroups A, C, W, and Y are high-molecular-weight carbohydrate polymers forming the outer capsule of the bacterium Neisseria meningitidis. These capsules are composed of repeating sugar units unique to each serogroup (A: (α1→6)-linked N-acetylmannosamine phosphate; C, W, Y: sialic acid-containing polysaccharides with serogroup-specific linkages) and serve as the primary basis for serogroup classification[7][10]. They protect the bacteria from host immune responses by inhibiting phagocytosis and complement-mediated lysis[7][9]. Vaccines targeting these antigens, especially when conjugated to carrier proteins, induce production of protective antibodies that mediate complement-dependent killing and opsonization, providing effective immunization against invasive meningococcal disease caused by these serogroups[7][3][10]. The measurement of serum antibodies against these polysaccharides can serve as a biomarker of vaccine-induced protection[3]. These antigens are not individual proteins or enzymes but rather polysaccharide structures, so they fall outside classical "drug targets" like receptors or enzymes, but they are the canonical molecular targets for several widely used vaccines, and measurement of antibody responses to them is a standard efficacy biomarker[3][9][10].

Other names
Meningococcal capsular polysaccharide (A, C, W, Y)MenA-C-W-Y antigenMeningococcal group A, C, W, Y antigens
02

Mechanism of action

Induction of antibody production leading to complement-mediated bacterial killing (serum bactericidal activity) Prevention of bacterial invasion by antibody-mediated opsonization

03

Biological functions

Immune evasion (by inhibiting host phagocytosis)Induction of protective immune response after vaccinationSerogroup differentiation/classification for epidemiology and diagnostics
04

Disease associations

Infection (driver of invasive meningococcal disease, including meningitis and septicemia)
05

Safety considerations

Poor immunogenicity of some polysaccharide antigens in young children, which led to development of protein-conjugated vaccinesRare risk of allergic reaction to vaccine componentsFor polysaccharide (not conjugate) vaccines: risk of hyporesponsiveness with repeated doses
06

Interacting drugs

Meningococcal conjugate vaccines (e.g., MenACWY conjugate vaccines)

1 more in the full profile.

07

Biomarkers

Serum bactericidal antibody titer (SBA) against serogroups A, C, W, YIgG concentration against specific capsular polysaccharide antigens

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